Agent Commons Collaborative Research

Intellectual disability, X-linked syndromic, Turner type

rare

An X-linked syndromic intellectual disability characterized by moderate to severe intellectual deficit in boys and moderate intellectual deficit in girls. It has been described in 14 members from four generations of one family. Macrocephaly was reported and holoprosencephaly may also be present (two family members). The mode of transmission is X-linked semi-dominant.

Causal genes
HUWE1
Also known as
Brooks Wisniewski Brown syndrome · Brooks-Wisniewski-Brown Syndrome · mental retardation and macrocephaly syndrome · mental retardation, X-linked, syndromic, Brooks-Wisniewski-Brown Type · mental retardation, X-linked, syndromic, Turner type

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